Staff Manufacturing Scientist

Wondering what's within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a significant career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.

The
Staff Manufacturing Scientist for Beckman Coulter is responsible for leading and supporting multi-site consumable manufacturing equipment validation and process improvement projects that deliver value to the company and meet cost, quality, and delivery objectives.

This position is an integral part of Consumable Sustaining Engineering and will be located in Chaska, MN and will be an onsite role. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time

You will work with the Senior Manager who is responsible for meeting quality, safety, and cost savings goals through design and manufacturing process improvements. If you thrive in a fast-paced and self-motivated role that applies a hands-on approach to plastics and equipment design and upgrades and want to work to build a world-class Integrated Supply Chain organization-read on!

In this role, you will have the opportunity to:

• Work with internal customers to identify consumable engineering improvement opportunities that support business growth.


• Work cross functionally to help define equipment user requirements, conduct risk analysis, draft verification and validation test plans and reports, and execute design transfers.


• Ensure compliance in the design and implementation of automated manufacturing equipment with the stated quality and engineering regulations in the medical device industry.


• Lead teams through design changes for technical processes or equipment improvement projects.

The essential requirements of the job include:

• Bachelor's degree in Biology or a related technical field with a minimum of 9+ years of relevant experience, or a Master's degree in a related field with at least 7+ years of relevant experience, or a Doctoral degree in a related field with a minimum of 4+ years of relevant experience.


• Demonstrated skills in design control processes, including design change, risk management, design requirements, design validation & verification, and design transfer.


• Experience in Project Management


• Experience working in GMP environment with automated manufacturing.

It would be a plus if you also possess previous experience in:

• Working knowledge of statistics


• Cell Culture Techniques

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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit

www.danaher.com
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We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.